Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome

Authors

Kristin Stawiarski, Yale New Haven Health Heart and Vascular Center, Bridgeport Hospital, Bridgeport, Connecticut.Follow
John-Ross D. Clarke, Yale New Haven Health Heart and Vascular Center, Bridgeport Hospital, Bridgeport, Connecticut.
Ari Pollack, Yale New Haven Health Heart and Vascular Center, Bridgeport Hospital, Bridgeport, Connecticut.
Robert Winslow, Yale New Haven Health Heart and Vascular Center, Bridgeport Hospital, Bridgeport, Connecticut.
Sachin Majumdar, Yale New Haven Health Heart and Vascular Center, Bridgeport Hospital, Bridgeport, Connecticut.Follow

Document Type

Article

Publication Title

HeartRhythm case reports

First Page

95

Last Page

99

DOI

10.1016/j.hrcr.2020.11.010

Publication Date

2-1-2021

Recommended Citation

Stawiarski, Kristin; Clarke, John-Ross D.; Pollack, Ari; Winslow, Robert; and Majumdar, Sachin, "Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome" (2021). Internal Medicine. 226.
https://scholar.bridgeporthospital.org/internal_medicine/226

Identifier

33665110 (pubmed); PMC7897746 (pmc); 10.1016/j.hrcr.2020.11.010 (doi); S2214-0271(20)30248-7 (pii)